Quaternary 3-aryl-7-triazinylamino-coumarin salts



United States Patent 3,518,266 QUATERNARY 3-ARYL-7-TRIAZINYLAMINO- COUMARIN SALTS Heinrich Hausermann, Riehen, and Eduard Troxler, Basel, Switzerland, assignors to Geigy Chemical Corporation, Ardsley, N.Y., a corporation of New York No Drawing. Filed July 23, 1968, Ser. No. 746,746 Claims priority, application Switzerland, July 25, 1967, 10,557/ 67 Int. Cl. C07d 55/20; C09k 1/02 US. Cl. 260249.6 7 Claims ABSTRACT OF THE DISCLOSURE Quaternary 3-aryl-7-[triazinyl-(2)-amino] coumarin salts are disclosed in which the carbon atom in 4-position in the triazinyl nucleus is substituted by a lower alkyl group, an optionally substituted lower alkoxy or lower alkylthio group, or an unsubstituted or organically substituted amino group, and the carbon atom in 6-position in the triazinyl nucleus is substituted by the grouping wherein Z represents an alkylene or oxa-alkylene bridge;

R represents hydrogen or a lower alkyl or alkenyl group;

R R and R represent certain organic substltuents; or

R and R together with the nitrogen atom represent certain heterocyclic radicals; or the grouping may represent a piperazinium radical, and which novel coumarins are useful for protecting foodstuifs and the like against the growth of Penicillium thereon; they are also useful for the optical brightening of acrylic fiber materials in unexpectedly high degrees of whiteness free from greenish hues; compositions containing the novel courmarins and a method of brightening acrylic fibers therewith are also described.

The novel compounds show also unexpectedly little tendency to precipitate from aqueous thiocyanate ioncontaining spinning baths for producing polyacrylonitrile filaments.

wherein A represents an optically non-chromogenically and nonionically substituted phenyl radical,

R and R independently of each other, each represent hydrogen or a lower alkyl group,

3,518,266 Patented June 30, 1970 R represents hydrogen or an optically substituted lower alkyl or lower alkenyl group,

R represents an optionally substituted lower alkyl or lower alkenyl group, a cycloalkyl or aralkyl radical,

Or R and R together form an alkylene group of preferably from 2 to 3 carbon atoms,

Each of R and R independently of the other represents an optionally substituted lower alkyl or lower alkenyl group, a cycloalkyl or aralkyl radical,

Or R and R taken together with the nitrogen atom to which they are linked represent a non-aromatic heterocycle radical which optionally includes an oxygen atom as ring member, all remaining ring members being preferably methylene groups;

X represents a lower alkyl group, an optionally substituted lower alkoxy or alkylthio group, or an amino radical of the formula wherein R, represents hydrogen or an optionally substituted lower alkyl or lower alkenyl group, and

R represents hydrogen, an optionally non-ionically and non-chromogenically substituted alkyl or phenyl radical, or lower alkenyl group, or

R and R together with the nitrogen to which they are linked, optionally with the inclusion of an oxygen atom as ring member, form a non-aromatic heterocycle,

Z represents an alkylene or oxa-alkylene radical, and

Y- represents the anion of a strong acid not having dyestuff character, ie the anion of an acid having at 18 C. a degree of dissociation of about 20% or higher and not imparting color to the coumarin derivatives of Formula I.

Suitable as substitutents of the alkyl groups R R R R R and R as well as of the alkoxy and alkylthio groups represented by X are the hydroxyl or a lower alkoxy group or halogen. Other substitutents of alkyl groups R R and R can be the cyano group, the carbamoyl or an alkoxy-carbonyl or hydroxy-alkoxy group.

In preferred compounds falling under Formula I A represents a phenyl radical any substituent of which is selected from lower alkyl, lower alkoxy and halogen of an atomic number of at most 35,

Each of R and R represents hydrogen or lower alkyl,

R represents hydrogen, lower alkyl or hydroxy-lower alkyl,

Each of R R and R represents, independently (a) Alkyl of from 1 to 6 carbon atoms, e.g. methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl or hexyl; or

(b) A substituted lower alkyl radicals any substituent of which is selected from lower alkoxy, carbamoyl, cyano, lower alkoxy-carbonyl, hydroxy-lower alkoxy or a phenyl radical any substituent of which is selected from lower alkyl and halogen of an atomic number of at most 35; e.g. Z-hydroxy-ethyl or 2-hydroxyor 3-hydroxypropyl; Z-methylethyl, Z-ethoxyethyl, 3-methoxypropyl; benzyl, methylbenzyl or chlorobenzyl; or

(c) Cycloalkyl, especially cyclohexyl or methylcyclohexyl; or

represents a trivalent piperazinium residue Or R and R taken together with the nitrogen atom to which they are linked represent pyrrolidino, piperidino, morpholino, hexahydroazepino, or lower alkyl morpholino;

X represents lower alkyl, lower alkoxy, lower alkyl- 5 thio, or a grouping wherein each of R and R represents hydrogen, alkyl of at most 6 carbon atoms, hydroXy-lower alkyl, hydroxy-lower alkoxy-lower alkyl, cyano-lower alkyl, carbamoyl-lower alkyl, cyclohexyl, lower-alkyl cyclohexyl, lower alkeny, or a phenyl amino radical any substitutent of which is selected from lower alkyl, lower alkoxy and halogen of an atomic number of at most 35, or

R and R together with the nitrogen atom to which they are linked represent pyrrolidino, piperidino, hexahydroazepino, morpholino or lower alkyl-morpholino,

Z represents divalent ethylene or propylene, and

Y- represents the anion of an acid having at 18 C. a degree of dissociation of about 20% or higher, and not imparting to the compounds of Formula I color, or to Penicillium growth-inhibiting amounts of said compounds toxicity to warm-blooded animals.

In the most-preferred compounds of Formula I A represents an unsubstituted phenyl radical, each of R and R represents hydrogen,

R represents hydrogen, lower alkyl or hydroxy-lower alkyl,

R represents lower alkyl, or

N -%N represents /N+ N- R and R represents lower alkyl, hydroxyalkyl of from 2 to 3 carbon atoms, alkoxyalkyl of a total of 3 to 5 carbon atoms, N(hydroxyalkyl) wherein alkyl alkoxy-carbonyl-lower alkyl, or carbamoyl-alkyl of a total of from 3 to 5 carbon atoms, or

R and R represents lower alkyl, hydroxyalkyl of to which they are linked represent pyrrolidino, piperidino, morpholino, hexahydroazepino or 2-monoor 2, 6-dimethylmorpholino,

X represents the same groupings as in the abovedescribed preferred dyestuffs, but more preferably the groupings NH -NH-lower alkyl, N(lower alkyl) --NH(hydroxyalkyl) wherein alkyl has from 2 to 3 carbon atoms, --NH(-(alkoxyalkyl) having a total of from 3 to 5 carbon atoms, .N (hydroxyalkyl) wherein alkyl has from 2 to 3 carbon atoms, --NH-(hydroxyalkoxyalkyl) of from 3 to 5 carbon atoms,

I CH3 methylphenylamino, chlorophenylamino, methoxyphenyl- 75 amino, pyrrolidino, piperidino, morpholino or Z-methylor 2,6-dimethyl-morpholino;

Z represents the ethylene or the 1,3-propylene group; and

Y represents one equivalent of a chlorine or bromine anion, or a, preferably lower, alkylsulfate or arylsulfonate anion, tag. the methosulfate or the p-toluene sulfonate anion, or a zinc-trihalide anion.

The term lower when used in this specification and the appended claims in connection with an aliphatic radical means that such radical has not more than 4, and preferably not more than 2 carbon atoms.

The new quaternary compounds form yellowish, water-soluble powders, the diluted aqueous solutions of which have a vivid blue fluorescense in daylight.

They are useful, due to their specific growth-inhibiting action on Penicillium strains, their very low toxicity to warm-blooded animals, and their lack of smell, for the control of such fungal growth on foodstuffs, e.g. preserves, such as marmalade, strawberry jam and the like, cheese of the type on which Penicillium growth is undesirable, e.g. Swiss cheese, Edam cheese and the like, as wellas on fruits.

Therefore, the invention provides, in another aspect, Penicillium growth-inhibiting and food preserving agents containing a compound according to the invention as active ingredient, and a method of inhibiting the growth of Penicillium strains, particularly on foodstuffs, by applying to the surface of the food an effective amount of a compound according to the invention.

The new quaternary salts are particularly valuable as active substances in preserving agents which are used, e.g. for citrus fruits such as grapefruit, oranges, lemons, also bananas, pineapple, avocados, mango, guajava, litchi, nut kernels, apples, pears, peaches, apricots, plums, grapes, strawberries, guava, sweet potatoes, potatoes, yams, carrots, turnips, sugar beet, onions, lettuce, artichokes, cabbage, asparagus, edible mushrooms, etc. In addition, these salts also have the other properties required of active substances for food preservatives, i.e. in the concentration necessary to preserve foodstuffs they are non-toxic to warm-blooded animals and they have no adverse effect on the taste and smell of the foodstuff, The salts are practically neutral compounds and they do not alter the pH of the substrate.

The preserving agents according to the present invention are applied in an amount of from about 0.005 to about 2.0, preferably about 0.01 to about 0.5 milligram per square centimeter of the surface of the fruit, plant or plant part to be treated.

The fungitoxic action of the new salts was determined by the so-called spore germination test on Penicillium spec., Penicillium digitatum, Penicillium italicum and Penicillium cyclopium.

For instance, one milliliter of a 1%, and in another test, a 0.5% solution of the compound of the formula OSOBCHa" was placed on 2 glass slides (26 x '76 mm.) under the same conditions. The solvent was evaporated off and a uniform coating of active substance was obtained on the glass slides. The slides were inoculated with spores of Penicillium strain and then kept in dishes at room temperature in an atmosphere which was almost saturated with steam. The germinated spores were counted for 24 hours, and the results were summarized in the following table.

TABLE Concentrate, g. per 100 ml. solu- Penicilliurn strain Compound tion (percent) Spec. Digitatum Italicum Cyclopiunl Quaternary compound of Formula Ia-.. 1 0.5 XXX XXX XXX XXX 1.0 XXX XXX XXX XXX Unquaternized compound corresponding 2 0.5 X

to that of Formula I. 2 1.0 X X XX4 X 1 In ethanol.

2 In acetone.

3 XXX=100% growth inhibition.

4 XX =50% growth inhibition.

5 X growth inhibitions.

Fruit and other edible parts of plants as well as other EMULSION CONCENTRATE foods are preserved according to the invention by pro- Parts viding them with a protective coating of the new com- The compound of Formula Ia 10 pound by either dipping, spraying, washing or painting Ethoxyethanol 15 them with liquid or waxy preparations containing a Dlmethyl formamide 15 Pencillium growth-inhibiting amount of active substances. In many cases, because of their advantageous solubility in water, the new food-protecting salts can be used in the form of aqueous solutions. On the other hand, it is possible to mix the active substances together with suitable non-injurious dispersing agents such as vegetable oils, fats or waxes and to use these dispersible preparations as aqueous or anhydrous dispersions.

Solvents suitable for use in such dispersions are nontoxic, low boiling, organic solvents such as low-molecular hydrocarbons, such as pentane, hexane, ketones, alcohols and ethers, such as methoxy-ethanol or ethoxyethanol.

It is of particular advantage in this aspect of the invention that the new compounds have strong blue fluorescence when irradiated with ultraviolet light. Due to this fact, it is easy to control whether application of the preserving agent, for instance on fruit such as apples, pears, oranges and the like has been uniform by passing the treated fruit on a conveyor belt or the like under an ultraviolet lamp. Insuflicicntly treated fruit can thus be detected instantaneousy and removed for renewed treatment.

The invention further provides compositions for the inhibition of penicillium growth, and especially for the treatment of food, which contain as active ingredient a compound falling under the first aspect of the invention in a Penicillium growth-inhibiting amount and a nontoxic, edible carrier therefor.

A paste, a pulverulent concentrate, an emulsion concentrate and a wax are described below; where not expressly stated, parts and percentages are by weight. Temperatures are given in degrees centigrade.

PASTE Parts The compound of Formula Ia A 1% aqueous hydroxyethyl cellulose solution 20 Ditertiary acetylene glycol 3 Distilled water 57 are milled and homogenised in a mixer into a thinly flowing 20% paste. On direct addition to water, the paste forms a milky dispersion. Freshly harvested oranges are dipped into a 1% dispersion and allowed to drip dry. About 0.01 to 0.1 mg. of active substance remained on the fruit per cm? surface. It was observed that the fruit showed no damage whatever do to micro-organisms after several days.

PULVERULENT CONCENTRATE 95 parts of the compound of Formula Ia and 5 parts of a condensation product of nonylphenol and ethylene oxide (molar ratio 1:9 to 1:10) or another suitable, preferably non-ionic, wetting agent are homogenised and finely milled in a suitable mill. This pulverulent concentrate is not dusty and quickly dissolves in water. A suspension, in 1% concentration, evenly wets fruit treated therewith.

Emulsifying agent consisting of a mixture of calcium dodecylbenzene sulphonate and the condensation product of nonylphenol and ethylene oxide (molar ratio about 1:8 to 1:10) 10 Petroleum (boiling range 230-270") 50 This mixture is a 10% emulsion concentrate which can be diluted with water to form emulsions of any concentration desired.

A 1% aqueous emulsion is used for the treatment of mould (e.g. Pencillium iza-Ifcum) on grapefruit. For this purpose, the fruit is dipped in the emulsion and left there for a few seconds. It is then allowed to drip dry. About 0.01 to 0.1 mg. of active substance remains on the fruit per crn. surface. The emulsion can also be sprayed on to the grapefruit or the latter can be washed therewith or can be applied thereto with a brush. The attack by Penicillium is greatly reduced by this treatment and any new infection is prevented.

PARRAFIN BLOCKS 890 parts of melted soft parafiin (M.P. 4l-43) are mixed with 100 parts of paraffin oil at about 60, and 10 parts of very finely ground (average particle size 20-50 microns) compound of Formula Ia are worked in until a homogeneous substance is obtained, which is poured into forms and then allowed to harden.

The resulting blocks are then used in a molten state in suitable apparatus, with slight heating, to coat citrus fruit with a thin film of the compound of Formula Ia sulfate in paraffin and thus protect them against spoilage. This apparatus may wax the surface of the citrus fruit e.g. by a rubbing action.

The consistency of the blocks can be varied as desired by increasing the amount of paraffin oil and also optionally adding surfactants such as sorbitan fatty acid esters, e.g. sorbitan-sesquioleate, sorbitan-monooleate, sorbitantrioleate, polyoxyethylene-sorbitan fatty acid esters, to obtain an increasingly softer block, thus adjusting the consistency to the requirements of the particular coating apparatus used.

PARAFFIN EMULSION 440 parts of soft parafiin (M.P. 41-43), 220 parts of parafiin oil, and 50 parts of Arlacel 83 (sorbitan-sesquioleate) are melted together while stirring at 5060. A hot solution of 300 parts of distilled water and 10 parts of the compound of Formula Ia is stirred into the melt, which is still warm (50), with a suitable Stirring apparatus (e.g. a Homorex-mixer) until a homogeneous substance is obtained.

The resulting water-in-oil emulsion is stirred while allowing to cool to about 30. A creamy substance of soft consistency is obtained, which can be applied in suitable apparatus, eg, by brushing, or lightly rubbing the peel of citrus fruit.

The concentration of active substance in the composition can also be varied (e.g. 0.5% or 1.5%). In lieu of Arlacel 83, other paraffin emulsifying agents, e.g. mixtures 7 of Span 80 and 85 (sorbitan-monooleate and sorbitantrioleate) can be used as well as other inert substances suitable for preparing similar water-in-oil emulsions of end products having optimal consistency, whereby the consistency can be adapted to the requirements of the particular apparatus used for wax-coating the citrus fruit.

The term edible parts of plants as used in this specilication and the appended claims refers to edible blossoms, seeds, fruit, leaves, sprouts, roots, bulbs and/or tubers of plants.

The invention further provides, according to another aspect thereof, a method of using the novel quaternary compounds for the brightening of cellulose fibers, and particularly of polyacrylonitrile fibers.

Polymeric or copolymeric acrylonitrile substrates are treated in the usual way from an acid aqueous bath at a raised temperature. The polyacrylonitrile can also be treated in a swollen condition such as occurs in the production of polyacrylonitrile filaments in an aqueous precipitation bath, with aqueous solutions of optical brighteners according to the invention. The amount of optical brightener used in these solutions is 0.01 to 0.5% of the weight of the fibers. The goods-to-bath ratio in exhaustion brightening is preferably in the range of about 1:20 to 1:50.

Polymeric or copolymeric acrylonitrile fiber materials which are particularly suitable for brightening with the compounds according to the invention are especially fibers about 80 to 100% of which consist of polymeric acrylonitrile and which contain acid dyesites, more particularly sulfonic acid and/or carboxylic acid dyesites.

Polyacrylonitrile fibers used in the examples given, infra, are

(a) Fibers which have a polymerization number of about 35,000 and possess per 100 g. of fibers about 46 millimols of sulfonic acid groups and 17 millimols of carboxyl groups as dyesites, referred to hereinafter as Orlon type fibers; or

(b) Fibers having the same polymerization number and, per 100 g. of fibers, about 154 millimols of carboxylic acid groups as dyesites, referred to hereinafter as Courtelle type fibers.

It is a particularly unexpected advantage of the compounds according to the invention that brilliant neutral white shades free from greening or yellowing discolorations are produced on these acrylic fibers even when the compounds are applied in high concentrations, namely 0.2 to 0.3% calculated on the weight of the fibers, while using a goods-to-bath ratio of about 1:30 to 1:40.

For it is well known, e.g. from the article by J. Lanther on Priifung and Bewertung von optischen Aufhellern published in June 1964 in Fachorgan fiir Textilveredlung by Schweizerische Vereinigung von Farbereifachlenten, XIX, No. 6, page 469, that the optical brightening of white substrates, which always possess a natural yellowish hue, to a neutral white aspect is achieved with very small amounts of blue-fluorescent optical brightener, in the order of 0.001%, and that, with increasing brightener concentration initially more and more brilliant white effects are achieved, but only until an optimal value is reached. Upon further increase of the brightener concentration, no further improvement of the white effect is achieved, but on the contrary, a decrease in white eflect and an increasingly yellowish or greenish discoloration effect are noted.

This is true particularly for the known tertiary compounds from which the new quaternary salts are formed, when such tertiary compounds are used in concentrations above 0.1% of the weight of the treated fiber material.

The brightened polyacrylonitrile materials of the Courtelle and Orlon type obtained with the compounds according to the invention is distinguished by very good light-fastness, wash-fastness, transparency, ironing fastness, a pure blue-fluorescent white effect free from undesirable reddish or greenish tinges, and, especially on Orlon-type fibers, excellent fastness to chlorite bleaches.

Another advantage of the new compounds lies in their lack of sensitivity to rhodanide ions. Such sensitivity is of great importance when polyacrylonitrile is to be spun into filaments by the so-called rhodanide wet spinning process, in which the conventional optical brighteners, when added to the aqueous precipitation bath, tend to precipitate as the number of rhodanide ions in this precipitation bath increases.

When optical brighteners according to the invention are added to such bath they are not precipitated and the brightening effect is not lost in the finishing process.

The quaternised compounds according to the invention are produced by reacting a compound of the formula with a compound of the formula preferably at elevated temperature; the symbols A, R through R X, Z and Y in Formulas II and HI have the same meanings as in Formula I.

The starting materials for the coumarin derivatives of Formula II used in the above process most of which are known, can be readily produced by the methods described in French Pat. No. 1,209,964.

The reaction of a coumarin compound of Formula H with a compound of Formula III is preferably performed in a solvent which is inert to the reaction partners. Examples of such solvents are aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as methylene chloride, tetrachloroethylene, chlorobenzene, bromobenzene or dichlorobenzene, also nitrobenzene, low alkanols and open and cyclic ethers such as ethanol, isopropanel, butanol, diethyl ether, dibutyl ether, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, tetrahydrofuran or dioxane; low ketones such as acetone or methylethyl ketone; fatty acid amides such as dimethyl formamide or dimethyl acetamide; sulphoxides such as dimethyl sulphoxide, and ureas such as tetramethyl urea.

If desired, the quaternary salts formed can be converted into other salts by double decomposition reaction.

The invention is further illustrated by the following non-limitative examples in which all temperatures are in degrees centigrade and all percentages are by weight.

Example 1 43.1 g. of 3 phenyl-7-[2-amino-4-(3 dimethylaminopropylamino)-s-triazinyl (6) amino]-coumarin are dissolved in 1000 ml. of anhydrous dioxane and, at 95-100, 16 g. of neutral dimethyl sulphate are added. The quaternary salt of the above formula then begins to separate out as a yellow oil which gradually crystallises. The mixture is stirred for another minutes at 100-105, then cooled. The methosulphate formed is filtered off. The product is washed well with ether and then dried in vacuo at The pale yellow crystals, which melt at 270 with decomposition, completely dissolve in water. The product also dissolves well in methanol and ethanol. The solutions fluoresce an intensive blue colour in daylight.

Its toxicity to worm-blooded animals is very low (DL for rats above 5000 mg./kg. bodyweight) In vitro tests have shown that the ethanolic solution of the final product in a concentration of 0.5 g. per ml. completely inhibits the growth of Penicillium strains, while the unquaternized starting compound, which must be applied in acetonic solution, fails to achieve satisfactory growth-inhibition even when used in a concentration of 1 g. in 100 ml.

The starting material used in this example, 3-phenyl-7- [2-amino-4-(3-dimethylamino-propylamino) s triaxinyl- (6)-amino1-coumarin, M.P. 215-217", is produced from 3-phenyl-7-[2-amino 4 chloro 1,3,5 triazinyl (6)- amino]-coumarir1 by reaction with excess N,N-dimethylpropylenediamine.

Example 2 l ICH2CHzCHzNH C-N OH:

g. of 3 phenyl-7-[2-diethylamino-4-(3-dimethylaminopropylamino)-s-triazinyl-(6)-amino] coumarin are dissolved by heating in 1000 ml. of chlorobenzene, 40 g.

of neutral dimethyl sulphate are added while stirring at 9095 and the mixture is kept for another 20 minutes at 90-95 The reaction product separates out as a yellowish, heavy oil which solidifies on cooling into a viscous mass. The chlorobenzene solution is decanted, another 1000 ml. of fresh chlorobenzene are added, the whole is again heated to 90-95 stirred well and the chlorobenzene phase, which is colourless for all practical purposes, is again decanted. The crude methosulphate remaining in the reaction vessel is dried in vacuo at 80-85". A yellow, Water soluble powder is obtained which has properties similar to the methosulphate obtained according to Example 1. The melting point is between 140-150. On boiling up with methylethyl ketone, a more crystalline product which melts at 148150 is obtained.

The 3-phenyl-7- [2-dimethylamino-4-( 3-dimethylaminopropylamino)-s-triazinyl-(6)-amino]-coumarin, M.P. (from ligroin), used as starting material in this example is produced in the usual way from 3 phenyl 7 aminocoumarin, cyanuric chloride, diethylamine and N,N-dimethylpropylenediamine.

The compounds which fall under the formula and the substituents of which are listed in the respective columns of the following table can be produced analogously. They are similarly useful for the optical brightening of polyacrylonitrile fibers, and for irmibiting the growth of Penicillium strains.

TABLE 1 Ex. X Q63 Aryl Y ZHS CH3 9 a- N- ppcmonmrr- Phenyl 011.504

CH5 CH3 CH3 or1 e 0 N ITICHZCHZOHZNH Phenyl onasol CH3 CH3 6B/ N- CH3-N N- Phenyl omso. C2115 CH3 G e /N HOCHZCHZN N-- Phenyl omsoi C2115 H3 7 H,N o N-omomomNH- Phenyl (111 50,

NCH2CH2NH- e 8 O2H5NH CH3 l Phenyl 01 \B e OH3NH N-OHZCHZNH- Phenyl cn so 1 CH CH 1 1 TABLE I-C0nt1nued Q Aryl Y 10 CH 0 l 9 a CIIZCHZCHZNH Phenyl 0113504 cm H; P

11 CH3- Same as above Pheuyl 011 804 12---- CH3OCH2CHZNH ao 2-chloropheny1 onasoa 13 O N d0 3,4-dich10rophcny1 011 80 14 HO GH CH NH- \NGZ CHZCH2CHZNH 4-metl1y1phe11y1 131- 15..." HzN' CH3 Pheuyl 9 -CHzCHzGHzNHE- C1 cgmomoooom 16 H N- CH3 Phenyl e \%CH2CHzCH2NH- C1 CH3 CHQCONHB 17 C2115 CH3 Phenyl \N- l ?C H2 C HzNH- 016 c515 0113 H CH CN 18. 01115 0H3 Phenyl e N- NCH2CH2NH (lg H5 ogHzcHzooHa 19..." CH2=CH-CH2NH CH9 Phenyl omso CHZCHZNH- OQJOH; 2o cNomomN- CH3 Phenyl CH3SO49 H3 -OH OH CHzNH- CH3 CH3 21 GHFOIL-Og; (w g-OH CH NIP Phenyl oHaso 2 2 GH2=CHO; cgc um 22 CNOHZOHZ Same as above Phenyl clztaso \N oNcmcfi, 23".-- 01130 011mm .-do Phenyl 011 80 omo smo 24... 1100111011, -do Phenyl cmso,

\N nocmcz 25..." do Phenyl 011 80 OH; 26.... oH3--NH -CHzCHq-NIL- Phenyl oHasor 27--.. NH Same as above Phenyl 0113504- 2s @NH- do Phenyl omso;

TABLE I-'C0ntinued EX. X Aryl Y OH; I ea 44"". (OH -(l3HCHz)zN- CH3- l ICHzCH2NH 3,4dimethy1phenyl Br- OH CH 6) 45. 021158 CH IIICHz-CH -CH2NH- P11011311 CH3SO4' 46. OHO- Same as above Phenyl 011 -80;-

47"... CzHr d0 Phenyl OK -SO 69 48". CzH5O- CH N-CHzCHzNH Phenyl CH3SO4" 49 NH3-C OOHN Same as above lhenyl Gil -SO 50 CzH5-OCH2CH2-NH- ..d0 H Pheuyl GHQ-SO4- 51 HO (CH2)3NH d0 Phenyl CH SOr CH3 lea 52- CH O-(CH )-NH 0H --N-cHtOHzCH2NH- Phenyl CR -SO4- 53 HO-CHzCH2-O Same as above .t Phenyl GH -604- CHzCHzNH- HOCHzCH2\ 54... /N-- .....do Phenyl CHg-SOF 55"... NH2COCH2-NH- d0 lllonyl Gila-SO4- Example 5 6 is produced by repeating Example 3 of U8. Pat. 2,945,033 The compound f the f l but using in lieu of 7-amino-3-phenyl-coumarin 25.1 CH3 parts of 7-amino-4-methyl-3-phenyl-coumarin obtained 0 according to Example 20 of U.S. Pat. 3,322,794. 4: The above compound is then first reacted with N,N-dimethylpropylenediamine and then quaternized as de- N C-NH scrlbed 1n Example 2, supra.

\ O 50 The optical brightener of the formula I N(CzH5)2 is obtained.

Example 5 7 The compound of the formula which brightens polyacrylonitrile fibers a brilliant neutral white, is obtained by repeating Example 56, but using in lieu of 7-amino-4-methyl-3-phenyl-coumarin an identical amount of 7-amino-6-methyl-3 phenyl-coumarine obtained as described in Example 1 of U.S. Pat. 3,322,794, but using in lieu of 3-aminopl1enol an equivalent amount of 3-amino-4-methyl-phenol.

Example 58 20 g. of polyacrylonitrile yarn (of Orlon type fibers) are introduced into a 50 warm liquor which contains 0.01 g. of the optical brightener described in Example 2 and 1 g. of formic acid in 600 ml. of water. The temperature is raised within 1.5 minutes to 96-98 and the liquor is kept for 30 minutes at this temperature. The yarn is then rinsed, first with lukewarm and then with cold water, and dried. The material so treated has a beautiful white effect in daylight.

Similar brightening effects are obtained if, in the above example, 1 g. of formic acid is replaced by 2.4 g. of concentrated hydrochloric acid or by 0.6 g. of concentrated sulphuric acid.

Example 59 20 g. of polyacrylonitrile yarn (of Courtelle type fibers) are first rinsed at a temperature of 60 in 600 ml. of water containing 0.6 g. of a non-ionic washing agent of nonylphenol polyglycol ether with 8-15 ethyleneoxy groups per mole and 0.3 g. of acetic acid. The yarn is then introduced into a 60 hot liquor which contains 0.03 g. of the optical brightener described in Example 1, 0.6 g. of oxalic acid, 0.075 g: of sodium metabisulphite and 0.15 g. of a mixture of sodium tetraand sodium hexametaphosphate. The temperature of the liquor is raised to 9698 within 20 minutes and kept at this temperature for another 30 minutes.

The yarn is then washed, first with lukewarm and then with cold water, if desired it is subjected to a further finishing process with a cationic softener of the bisstearyl-bis-ethyl ammonium chloride type, and dried.

Yarn so treated has a very beautiful white effect in daylight.

Similar brightening effects are obtained if, in the above example, the optical brightener mentioned is replaced by about the same amounts of one of the compounds given in Examples 2 to 57 and otherwise the procedure given in the example is followed.

Example 60 A fabric made of Orlon type stable fibers is impregnated in a padding machine at 25 with a solution containing 2 g. of the optical brightener given in Example 1 in 1000 ml. of water. The fabric is dried at a temperature of 60 and then steamed for 15 minutes at 100-102. The fabric so treated has a very strong white effect.

Example 61 250 g. of an acrylic polymer, which is described below, is dissolved in 750 g. of N,N-dimethyl formamide contain ing 2.5 g. of titanium dioxide at 70 while stirring continuously and vigorously. This solution is spun through a spinneret having 500 holes (diameter 0.1 mm.) in a coagulation bath containing equal amounts of dimethyl formamide and 50 warm water. The resulting filaments are stretched by 450% in boiling water and then impregnated with optical brightener by passing the filaments through an aqueous bath which contains 500 ppm. of the optical brightener described in Example 1 in addition to acetous N,N distearoylaminoethyl-N,N'-dihydroxyethyl urea. The fibres are then dried at 120 and stabilised with steam at 120.

The acrylic polymer used in this example is produced as follows: a mixture of monomers is polymerized in a litre glass reaction vessel containing 1500 ml. of H 80 n/1000. After adjusting the pH to 2.5, the following solutions are introduced into the reaction vessel separately 18 and yet simultaneously, the additions being made within 2 hours at 50:

Mixture of monomers consisting of:

% acrylonitrile and 10% methyl acrylate-800 g. 2.5% aqueous Na S O solution-1000 ml.

0.5% aqueous K S O solutionl000 ml.

4% aqueous sulphuric acid solution-500 ml.

After a reaction time of 3 hours, the polymer is separated from the reaction mixture by filtration and washed with water. The copolymer having acid groups thus obtained which consists of 91% acrylonitrile and 9% methyl acrylate, has an intrinsic viscosity=l.5 deciliter/ gram and contains 4 milliequivalents per g. of fibers of sulfonic acid dyesites.

Example 62 250 g. of an acrylic polymer, the production of which is described below, are dissolved in 750 g. of N,N-dimethyl formamide containing 2.5 g. of titanium dioxide while stirring at 70. This solution is spun through a spinneret into a coagulation bath containing equal amounts of di methyl formamide and water. The filaments so spun are stretched by 450% in boiling water and then passed through an aqueous finishing bath at a rate of about 20 g. per minute, to which bath there is added optical brightener produced according to Example 2, at a rate of 20 mg. per minute, dissolved in the IOU-fold amount of water containing N,N'-distearoylaminoethyl-N,N-dihydroxyethyl urea acetate acting as softening and mildly antistatic agent. The fibers are then dried at and stabilized with steam at 120.

The acrylic polymer used in this example is produced as follows: A mixture of monomers is polymerised in a 5 litre glass reaction vessel containing 1500 ml. of N/ 1000 H 50 by introducing the following solutions into the reaction vessel within 2 hours at 20.

Mixture of monomers consisting of:

90% acrylonitrile and 10% methyl acry1ate-800 g.

0.85% aqueous H 0 solution960 ml.

2.1% aqueous Ti (SO solution containing 3.2%

H SO -960 ml.

1% aqueous solution of sodium vinylbenzene sulphomate-800 ml.

After a reaction time of 3 hours, 650 g. of a copolymer are obtained which consists of 91% acrylonitrile, 8% methyl acrylate and 1% vinylbenzene sulphonic acid, has an intrinsic viscosity of 1.55 deciliters per gram, and contains per 100 g. thereof, 4.8 milliequivalents of sulfonic acid groups.

We claim:

1. A compound of the formula:

wherein A represents an unsubstituted phenyl radical or a phenyl radical substituted with a member selected from lower alkyl, lower alkoxy and halogen of an atomic number of at most 35,

each of R and R represents hydrogen or lower alkyl,

R represents hydrogen, lower alkyl or hydroxy-lower alkyl,

each of R R and R represents a substituent selected from (a) alkyl of from 1 to -6 carbon atoms;

(b) a substituted lower alkyl radical wherein the substitutent is selected from lower alkoxy carbamoyl, cyano, lower alkoxy-carbonyl, hydroxylower alkoxy or a phenyl radical or a phenyl 19 radical substituted with a member selected from lower alkyl and halogen of an atomic number of at most 35; (c) cyclohexyl; and (d) lower alkyl-cyclohexyl; or

Formula I color, or to Penicillium growth-inhibiting amounts of said compound toxicity to warm-blooded animals. 2. A compound as defined in claim 1, which is of the formula $1! (13H: N-O CHaIlI-(CHz)aNHC \N H Re N=C NH \o/ wherein NZN 1R represents methyl or carbamoylmethyl,

R R3 X represents amino, di-(lower alkyl)-amino, methoxy or methyl, and represents a trivalent piperazlnlum residue represents or R and R taken together with the nitrogen atom to which they are linked represent pyrrolidino, piperidino, morpholine, hexahydroazepino, or lower alkylmorpholino; 2

X represents lower alkyl, lower alkoxy, lower alkylthio,

or a grouping wherein each of R and R represents hydrogen, alkyl of at most 6 carbon atoms, hydroxy-lower alkyl, hydroxy-lower alkoxy-lower alkyl, cyano-lower alkyl, carbamoyl-lower alkyl, cyclohexyl, loweralkyl-cyclohexyl, lower alkenyl, or a phenyl amino radical or a substituted phenyl aminoradical wherein the substituent is selected from lower alkyl, lower alkoxy and halogen of an atomic number of at most 35, or

R and R together with the nitrogen atom to which they are linked represent pyrrolidino, piperidino, hexahydroazepino, morpholine or lower alkyl-morpholino,

Z represents divalent ethylene or propylene, and

Y- represents the anion of an acid having at 180 C. a degree of dissociation of about 20% or higher, and not imparting to the compound or Zn Ch" 3. A compound as defined in claim 1, wherein R represents methyl and X" represents amino.

4. A compound as defined in claim 1, wherein R represents methyl and X" represents methoxy.

5. A compound as defined in claim 1, wherein R represents methyl and X" represents diethylamino.

6. A compound as defined in claim 1, wherein R represents methyl and X" represents methyl.

7. A compound as defined in claim 1, wherein R represents carbamoylmethyl and X" represents amino.

References Cited UNITED STATES PATENTS 2,945,033 7/1960 Hausermann 260249.8 X R 3,242,177 3/ 1966 Schellhammer et a1.

H-EN RY 1R. JILES, Primary Examiner I. M. FORD, Assistant Examiner US. Cl. X.R. 

